FDA UDI Not in Commercial Distribution 🇺🇸 United States

COUPLAND SUCTION TUBE SET

DI: B09941262SET9 · Model: 412-672-SET · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
COUPLAND SUCTION TUBE SET
Primary DI
B09941262SET9
Version / Model
412-672-SET
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2017-09-30
Public Version
4
Public Version Date
2018-09-28
Public Version Status
Update
Public Device Record Key
e011e333-6020-46ac-a255-fe1f1c88d64f
Distribution End Date
2018-09-28

Device Description

COUPLAND SUCTION TUBE SET

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
JOL Catheter And Tip, Suction

GMDN Terms

Code Name
45254 Suction cannula, reusable

Identifiers

Type ID
Primary B09941262SET9
Unit of Use B09941262SET05

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 6.50 Inch